Microinjections of muscimol into lateral superior colliculus disrupt orienting and oral movements in the formalin model of pain

An important reaction in rodent models of persistent pain is for the animal to turn and bite/lick the source of discomfort (autotomy). Comparatively little is known about the supraspinal pathways which mediate this reaction. Since autotomy requires co-ordinated control of the head and mouth, it is possible that basal ganglia output via the superior colliculus may be involved; previously this projection has been implicated in the control of orienting and oral behaviour. The purpose of the present study was therefore, to test whether the striato-nigro-tectal projection plays a significant role in oral responses elicited by subcutaneous injections of formalin. Behavioural output from this system is normally associated with the release of collicular projection neurons from tonic inhibitory input from substantia nigra pars reticulata. Therefore, in the present study normal disinhibitory signals from the basal ganglia were blocked by injecting the GABA agonist muscimol into different regions of the rat superior colliculus. c-Fos immunohistochemistry was used routinely to provide regional estimates of the suppressive effects of muscimol on neuronal activity. Biting and licking directed to the site of a subcutaneous injection of formalin (50 microliters of 4%) into the hind-paw were suppressed in a dose-related manner by bilateral microinjections of muscimol into the lateral superior colliculus (10-50 ng; 0.5 microliter/side); injections into the medial superior colliculus had little effect. Bilateral injections of muscimol 20 ng into lateral colliculus caused formalin-treated animals to re-direct their attention and activity from lower to upper regions of space. Muscimol injected unilaterally into lateral superior colliculus elicited ipsilateral turning irrespective of which hind-paw was injected with formalin. Oral behaviour was blocked when the muscimol and formalin injections were contralaterally opposed; this was also true for formalin injections into the front foot. Interestingly, when formalin was injected into the perioral region, injections of muscimol into the lateral superior colliculus had no effect on the ability of animals to make appropriate contralaterally directed head and body movements to facilitate localization of the injected area with either front- or hind-paw. These findings suggest that basal ganglia output via the lateral superior colliculus is critical for responses to noxious stimuli which entail the mouth moving to and acting on the foot, but not when the foot is the active agent applied to the mouth. The data also suggest that pain produces a spatially non-specific facilitation of units throughout collicular maps, which can be converted into a spatially inappropriate signal by locally suppressing parts of the map with the muscimol.

[1]  J. Deniau,et al.  Disinhibition as a basic process in the expression of striatal functions , 1990, Trends in Neurosciences.

[2]  J. Besson,et al.  A reinvestigation of the analgesic effects induced by stimulation of the periaqueductal gray matter in the rat. II. Differential characteristics of the analgesia induced by ventral and dorsal PAG stimulation , 1984, Brain Research.

[3]  T. Tsumori,et al.  Demonstration of axon collateral projections from the substantia nigra pars reticulata to the superior colliculus and the parvicellular reticular formation in the rat , 1995, Brain Research.

[4]  R. Mize,et al.  Immunocytochemical localization of gamma‐aminobutyric acid (GABA) in the cat superior colliculus , 1988, The Journal of comparative neurology.

[5]  P. Wall,et al.  Textbook of pain , 1989 .

[6]  P. Dean,et al.  Regional expression of fos-like immunoreactivity following seizures induced by pentylenetetrazole and maximal electroshock , 1992, Experimental Neurology.

[7]  P. Wall,et al.  Pain mechanisms: a new theory. , 1965, Science.

[8]  B E Stein,et al.  Nociceptive neurons in rat superior colliculus: response properties, topography, and functional implications. , 1989, Journal of neurophysiology.

[9]  J M Groh,et al.  Saccades to somatosensory targets. II. motor convergence in primate superior colliculus. , 1996, Journal of neurophysiology.

[10]  D. Dubuisson,et al.  The formalin test: A quantitative study of the analgesic effects of morphine, meperidine, and brain stem stimulation in rats and cats , 1977, Pain.

[11]  John H. Martin Autoradiographic estimation of the extent of reversible inactivation produced by microinjection of lidocaine and muscimol in the rat , 1991, Neuroscience Letters.

[12]  Alan C. Evans,et al.  Distributed processing of pain and vibration by the human brain , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[13]  R. Mize,et al.  The neurons of the substantia nigra and zona incerta which project to the cat superior colliculus are GABA immunoreactive: A double-label study using GABA immunocytochemistry and lectin retrograde transport , 1989, Neuroscience.

[14]  P. Dean,et al.  Locomotor activity of rats in open field after microinjection of procaine into superior colliculus or underlying reticular formation , 1982, Behavioural Brain Research.

[15]  R. F. Westbrook,et al.  The formalin test: scoring properties of the first and second phases of the pain response in rats , 1995, Pain.

[16]  J. C. Liter,et al.  Evidence that the substantia nigra is a component of the endogenous pain suppression system in the rat , 1988, Brain Research.

[17]  P. Redgrave,et al.  Analysis of nociceptive neurones in the rat superior colliculus using c‐fos immunohistochemistry , 1996, The Journal of comparative neurology.

[18]  A. Depaulis,et al.  Suppressive effects of intranigral injection of muscimol in three models of generalized non-convulsive epilepsy induced by chemical agents , 1989, Brain Research.

[19]  E. Chudler,et al.  The role of the basal ganglia in nociception and pain , 1995, Pain.

[20]  B. Stein,et al.  The Merging of the Senses , 1993 .

[21]  D. Price,et al.  Patterns of increased brain activity indicative of pain in a rat model of peripheral mononeuropathy , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[22]  J. Gentle,et al.  Randomization and Monte Carlo Methods in Biology. , 1990 .

[23]  J. Deniau,et al.  The lamellar organization of the rat substantia nigra pars reticulata: Distribution of projection neurons , 1992, Neuroscience.

[24]  P. Dean,et al.  Organization of the crossed tecto-reticulo-spinal projection in rat—I. Anatomical evidence for separate output channels to the periabducens area and caudal medulla , 1990, Neuroscience.

[25]  A. Routtenberg,et al.  Histochemical Fluorescence after Application of Neurochemicals to Caudate Nucleus and Septal Area in vivo , 1968, Science.

[26]  J. Bolam,et al.  Monosynaptic innervation of trigeminal motor neurones involved in mastication by neurones of the parvicellular reticular formation , 1993, The Journal of comparative neurology.

[27]  Karl J. Friston,et al.  Cortical and subcortical localization of response to pain in man using positron emission tomography , 1991, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[28]  D. Sparks,et al.  Saccades to somatosensory targets. I. behavioral characteristics. , 1996, Journal of neurophysiology.

[29]  R. Raghupathi,et al.  Cellular Responses to Experimental Brain Injury , 1995, Brain pathology.

[30]  Barry E. Stein,et al.  Eye movements evoked by electrical stimulation in the superior colliculus of rats and hamsters , 1982, Brain Research.

[31]  G. Holstege,et al.  Brainstem-spinal cord projections in the cat, related to control of head and axial movements. , 1988, Reviews of oculomotor research.

[32]  Charles Nicholson,et al.  Diffusion from an injected volume of a substance in brain tissue with arbitrary volume fraction and tortuosity , 1985, Brain Research.

[33]  P. Dean,et al.  Tonic desynchronisation of cortical electroencephalogram by electrical and chemical stimulation of superior colliculus and surrounding structures in urethane-anaesthetised rats , 1985, Neuroscience.

[34]  J Schouenborg,et al.  Climbing fibres projecting to cat cerebellar anterior lobe activated by cutaneous A and C fibres. , 1987, The Journal of physiology.

[35]  P. Dean,et al.  Tectal induction of cortical arousal: Evidence implicating multiple output pathways , 1991, Brain Research Bulletin.

[36]  R. Wurtz,et al.  Modification of saccadic eye movements by GABA-related substances. I. Effect of muscimol and bicuculline in monkey superior colliculus. , 1985, Journal of neurophysiology.

[37]  G. E. Alexander,et al.  Functional architecture of basal ganglia circuits: neural substrates of parallel processing , 1990, Trends in Neurosciences.

[38]  M. Pisa Motor somatotopy in the striatum of rat: Manipulation, biting and gait , 1988, Behavioural Brain Research.

[39]  R. Wurtz,et al.  Role of the basal ganglia in the initiation of saccadic eye movements. , 1986, Progress in brain research.

[40]  S. Charpier,et al.  The lamellar organization of the rat substantia nigra pars reticulata: Segregated patterns of striatal afferents and relationship to the topography of corticostriatal projections , 1996, Neuroscience.

[41]  P. Dean,et al.  Opposing Excitatory and Inhibitory Influences from the Cerebellum and Basal Ganglia Converge on the Superior Colliculus: an Electrophysiological Investigation in the Rat , 1994, The European journal of neuroscience.

[42]  X. Zhang,et al.  Spinohypothalamic tract neurons in the cervical enlargement of rats: descending axons in the ipsilateral brain , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[43]  J M Groh,et al.  Saccades to somatosensory targets. III. eye-position-dependent somatosensory activity in primate superior colliculus. , 1996, Journal of neurophysiology.

[44]  Joe C. Adams,et al.  Biotin amplification of biotin and horseradish peroxidase signals in histochemical stains. , 1992, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[45]  S. Hsu,et al.  The use of antiavidin antibody and avidin-biotin-peroxidase complex in immunoperoxidase technics. , 1981, American journal of clinical pathology.

[46]  M. Behan,et al.  Intrinsic circuitry in the deep layers of the cat superior colliculus , 1996, Visual Neuroscience.

[47]  J. Sonnenberg,et al.  Dynamic alterations occur in the levels and composition of transcription factor AP-1 complexes after seizure , 1989, Neuron.

[48]  P Redgrave,et al.  Movements resembling orientation or avoidance elicited by electrical stimulation of the superior colliculus in rats , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[49]  S. Hunt,et al.  Induction of c-fos-like protein in spinal cord neurons following sensory stimulation , 1987, Nature.

[50]  G. Collingridge,et al.  Evidence for the participation of nigrotectal γ-aminobutyrate-containing neurones in striatal and nigral-derived circling in the rat , 1982, Neuroscience.

[51]  A. Woda,et al.  The orofacial formalin test in rats: effects of different formalin concentrations , 1995, Pain.

[52]  R. Melzack,et al.  The formalin test: a validation of the weighted-scores method of behavioural pain rating , 1993, Pain.

[53]  K. Nakano,et al.  Descending projections from the superior colliculus to the reticular formation around the motor trigeminal nucleus and the parvicellular reticular formation of the medulla oblongata in the rat , 1994, Brain Research.

[54]  M. Dubach Distribution of intracerebrally injected dopamine as studied by a punch-scintillation modeling technique , 1991, Neuroscience.

[55]  E. Chudler,et al.  Nociceptive responses in the neostriatum and globus pallidus of the anesthetized rat. , 1993, Journal of neurophysiology.

[56]  P. Redgrave,et al.  Chapter 24 Functional anatomy of nociceptive neurones in rat superior colliculus , 1996 .

[57]  P. Dean,et al.  Differential expression of fos-like immunoreactivity in the descending projections of superior colliculus after electrical stimulation in the rat , 1996, Behavioural Brain Research.

[58]  T. Curran,et al.  Stimulus-transcription coupling in the nervous system: involvement of the inducible proto-oncogenes fos and jun. , 1991, Annual review of neuroscience.

[59]  Y. Smith,et al.  Synaptic organization of gabaergic inputs from the striatum and the globus pallidus onto neurons in the substantia nigra and retrorubral field which project to the medullary reticular formation , 1992, Neuroscience.

[60]  P. Gass,et al.  Basal expression of the inducible transcription factors c‐Jun, JunB, JunD, c‐Fos, FosB, and Krox‐24 in the adult rat brain , 1995, The Journal of comparative neurology.

[61]  C. Gerfen The neostriatal mosaic: multiple levels of compartmental organization in the basal ganglia. , 1992, Annual review of neuroscience.

[62]  S. Barasi Responses of substantia nigra neurones to noxious stimulation , 1979, Brain Research.

[63]  P. Dean,et al.  Event or emergency? Two response systems in the mammalian superior colliculus , 1989, Trends in Neurosciences.

[64]  A. Aloisi,et al.  Behavioural effects of different intensities of formalin pain in rats , 1995, Physiology & Behavior.

[65]  C. Porro,et al.  Functional activity mapping of the rat brainstem during formalin-induced noxious stimulation , 1991, Neuroscience.

[66]  G. Giesler,et al.  Spinothalamic and spinohypothalamic tract neurons in the cervical enlargement of rats. I. Locations of antidromically identified axons in the thalamus and hypothalamus. , 1994, Journal of neurophysiology.

[67]  M. Segraves,et al.  Acute activation and inactivation of macaque frontal eye field with GABA-related drugs. , 1995, Journal of neurophysiology.

[68]  P. Dean,et al.  Reduced locomotor activity as an acute effect of damage to superior colliculus in rats , 1984, Behavioural Brain Research.

[69]  G. Paxinos,et al.  The Rat Brain in Stereotaxic Coordinates , 1983 .

[70]  A. Cowan,et al.  Naloxone causes apparent antinociception and pronociception simultaneously in the rat paw formalin test. , 1993, European journal of pharmacology.

[71]  Barry E. Stein,et al.  Superior colliculus cells respond to noxious stimuli , 1978, Brain Research.

[72]  D. Hubel,et al.  Topography of visual and somatosensory projections to mouse superior colliculus. , 1976, Journal of neurophysiology.

[73]  P. Dean,et al.  Topographical organization of the nigrotectal projection in rat: Evidence for segregated channels , 1992, Neuroscience.

[74]  P. Dean,et al.  Regional Distribution of the Anticonvulsant and Behavioural Effects of Muscimol Injected into the Substantia Nigra of Rats , 1996, The European journal of neuroscience.

[75]  P. Dean,et al.  Behavioural consequences of manipulating GABA neurotransmission in the superior colliculus. , 1992, Progress in brain research.

[76]  R. Faull,et al.  Induction of c-fos mRNA and protein in neurons and glia after traumatic brain injury: Pharmacological characterization , 1990, Experimental Neurology.

[77]  J. Deniau,et al.  Spatio-temporal organization of a branched tecto-spinal/ tecto-diencephalic neuronal system , 1984, Neuroscience.

[78]  P. Dean,et al.  Bypassing the Saccadic Pulse Generator: Possible Control of Head Movement Trajectory by Rat Superior Colliculus , 1991, The European journal of neuroscience.

[79]  P. Dean,et al.  Superior colliculus lesions selectively attenuate apomorphine-induced oral stereotypy: a possible role for the nigrotectal pathway , 1980, Brain Research.

[80]  C. Gerfen The neostriatal mosaic. I. compartmental organization of projections from the striatum to the substantia nigra in the rat , 1985, The Journal of comparative neurology.

[81]  S. P. Hunt,et al.  Changing patterns of c-fos induction in spinal neurons following thermal cutaneous stimulation in the rat , 1990, Neuroscience.